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rs796052616

From SNPedia

Orientationminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs796052616(C;T)
Make rs796052616(T;T)
ReferenceGRCh38.p2 38.2/147
Chromosome20
Position63446796
GeneKCNQ2, LOC105372720
is asnp
is mentioned by
dbSNPrs796052616
ebirs796052616
HLIrs796052616
Exacrs796052616
Varsomers796052616
Maprs796052616
PheGenIrs796052616
hapmaprs796052616
1000 genomesrs796052616
hgdprs796052616
ensemblrs796052616
gopubmedrs796052616
geneviewrs796052616
scholarrs796052616
googlers796052616
pharmgkbrs796052616
gwascentralrs796052616
openSNPrs796052616
23andMers796052616
23andMe allrs796052616
SNP Nexus

SNPshotrs796052616
SNPdbers796052616
MSV3drs796052616
GWAS Ctlgrs796052616
Max Magnitude0
ClinVar
Risk rs796052616(T;T)
Alt rs796052616(T;T)
Reference rs796052616(C;C)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene KCNQ2
CLNDBN not provided
Reversed 1
HGVS NC_000020.10:g.62078149G>A
CLNSRC
CLNACC RCV000187850.1,